rs121907996(A;G)

Carrier of a Wilson disease mutation

Is a	genotype
of	rs121907996
Gene	ATP7B
Chromosome	13
Position	51,946,438
mentioned	by

Magnitude

3

Repute

Bad

Geno	Mag	Summary
(A;G)	3	Carrier of a Wilson disease mutation
(G;G)	0	common in clinvar

Unaffected in absence of a second ATP7B gene mutation